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Catalog Number:
15667
CAS Number:
501015-34-5
Acide Fmoc-( S -3-amino-3-(2,4-dichlorophényl)propionique)
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-β-Phe(2,4-DiCl)-OH, ( S -Fmoc-2,4-Dichloro-β-phénylalanine
Documents
$106.96 /250 mg
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Product Information

Fmoc-(S)-3-amino-3-(2,4-dichlorophenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound, recognized for its unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, facilitates the efficient assembly of peptides by providing stability during the synthesis process. Its specific structure, featuring a dichlorophenyl moiety, enhances its potential for biological activity, making it an attractive candidate for drug development and research applications.

Researchers and industry professionals can leverage this compound in the design of novel peptides with targeted therapeutic effects, particularly in the fields of oncology and neuropharmacology. Its ability to improve solubility and bioavailability compared to similar compounds positions it as a valuable asset in pharmaceutical formulations. Whether you are developing new therapeutic agents or conducting advanced research, Fmoc-(S)-3-amino-3-(2,4-dichlorophenyl)propionic acid offers significant advantages in efficiency and efficacy.

Synonyms
Fmoc-L-β-Phe(2,4-DiCl)-OH, ( S -Fmoc-2,4-Dichloro-β-phénylalanine
CAS Number
501015-34-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 24 H 19 Cl 2 NO 4
Molecular Weight
456.32
MDL Number
MFCD03427980
PubChem ID
22309348
Melting Point
182 - 184 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = - 8 ± 1° (C=1 dans DMF)
Conditions
Conserver à 0-8°C
General Information
Synonyms
Fmoc-L-β-Phe(2,4-DiCl)-OH, ( S -Fmoc-2,4-Dichloro-β-phénylalanine
CAS Number
501015-34-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 24 H 19 Cl 2 NO 4
Molecular Weight
456.32
MDL Number
MFCD03427980
PubChem ID
22309348
Melting Point
182 - 184 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = - 8 ± 1° (C=1 dans DMF)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(S)-3-amino-3-(2,4-dichlorophenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids. Its stability under various conditions makes it a preferred choice for researchers in the field of organic chemistry.
  • Drug Development: The compound's unique structure is beneficial in the design of novel pharmaceuticals, particularly in creating compounds with enhanced bioactivity and specificity for targeted therapies.
  • Bioconjugation: It is used in bioconjugation processes, enabling the attachment of biomolecules to drugs or diagnostic agents, which is crucial in developing targeted drug delivery systems.
  • Research in Neuroscience: The compound's derivatives are explored in neuroscience research for their potential role in modulating neurotransmitter systems, which could lead to advancements in treating neurological disorders.
  • Material Science: Its properties are also being investigated for applications in material science, particularly in creating functionalized polymers that can be used in various industrial applications.

Citations